A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3610882



Internal ID6997798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:134665935..134666570hg38UCSC Ensembl
Innerchr6:134665985..134666520hg38UCSC Ensembl
Outerchr6:134665885..134666620hg38UCSC Ensembl
chr6:134987073..134987708hg19UCSC Ensembl
Innerchr6:134987123..134987658hg19UCSC Ensembl
Outerchr6:134987023..134987758hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg38636
hg19636
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12559649, essv12559650
SamplesHG03696, HG03681
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3610882
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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